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Cancer Related Genes (PRLR)

a gene and gene technology, applied in the field of cancer-associated genes, can solve the problems of high cancer rate of infected animals and clustering, and achieve the effect of modulating the survival rate of cancerous cells and heightening the adcc activity

Inactive Publication Date: 2009-09-03
FANIDI ABDALLAH +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0033]Preferably, antibodies for therapeutic use in accordance with the invention are effective to elicit ADCC, and modulates the survival of cancerous cells by binding to

Problems solved by technology

In some models, uninfected animals have low cancer rates, and infected animals have high cancer rates.
This is because the genome is too large for random integrations to result in observable clustering.

Method used

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  • Cancer Related Genes (PRLR)
  • Cancer Related Genes (PRLR)
  • Cancer Related Genes (PRLR)

Examples

Experimental program
Comparison scheme
Effect test

example 1

Insertion Site Analysis Following Tumor Induction in Mice

[0432]Tumors were induced in mice using either mouse mammary tumor virus (MMTV) or murine leukemia virus (MLV). MMTV causes mammary adenocarcinomas and MLV causes a variety of different hematopoetic malignancies (primarily T- or B-cell lymphomas).

[0433]Three routes of infection were used: (1) injection of neonates with purified virus preparations,[0434](2) infection by milk-borne virus during nursing, and (3) genetic transmission of pathogenic proviruses via the germ-line (Akvr1 and / or Mtv2). The type of malignancy present in each affected mouse was determined by histological analysis of H&E-stained thin sections of formalin-fixed, paraffin-embedded biopsy samples. Host DNA sequences flanking all clonally-integrated proviruses in each tumor were recovered by nested anchored-PCR using two virus-specific primers and two primers specific for a 40 bp double stranded DNA anchor ligated to restriction enzyme digested tumor DNA. Ampl...

example 2

Analysis of Quantitative RT-PCR: Comparative CT Method

[0440]The RT-PCR analysis was divided into 4 major steps: 1) RNA purification from primary normal and tumor tissues; 2) Generation of first strand cDNA from the purified tissue RNA for Real Time Quantitative PCR; 3) Setup RT-PCR for gene expression using ABI PRISM 7900HT Sequence Detection System tailored for 384-well reactions; 4) Analyze RT-PCR data by statistical methods to identify genes differentially expressed (up-regulated) in cancer.

[0441]These steps are set out in more detail below.

A) RNA Purification from Primary Normal and Tumor Tissues

[0442]This was performed using Qiagen RNeasy mini Kit CAT#74106. Tissue chucks typically yielded approximately 30 μg of RNA resulting in a final concentration of approximately 200 ng / μl if 150 μl of elution buffer was used.

[0443]After RNA was extracted using Qiagen's protocol, Ribogreen quantitation reagents from Molecular Probes was used to determine yield and concentration of RNA accor...

example 3

Detection of PRLR-Sequences in Human Cancer Cells and Tissues

[0480]DNA from prostate and breast cancer tissues and other human cancer tissues, human colon, normal human tissues including non-cancerous prostate, and from other human cell lines are extracted following the procedure of Delli Bovi et al. (1986, Cancer Res. 46:6333-6338). The DNA is resuspended in a solution containing 0.05 M Tris HCl buffer, pH 7.8, and 0.1 mM EDTA, and the amount of DNA recovered is determined by microfluorometry using Hoechst 33258 dye. Cesarone, C. et al., Anal Biochem 100:188-197 (1979).

[0481]Polymerase chain reaction (PCR) is performed using Taq polymerase following the conditions recommended by the manufacturer (Perkin Elmer Cetus) with regard to buffer, Mg2+, and nucleotide concentrations. Thermocycling is performed in a DNA cycler by denaturation at 94° C. for 3 min. followed by either 35 or 50 cycles of 94° C. for 1.5 min., 50° C. for 2 min. and 72° C. for 3 min. The ability of the PCR to ampli...

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Abstract

This invention is in the field of cancer-associated genes. Specifically it relates to methods for detecting cancer or the likelihood of developing cancer based on the presence or absence of expression of a PRLR gene or protein. The invention also provides methods and molecules for upregulating or downregulating PRLR gene expression and PRLR protein activity.

Description

[0001]This application claims the benefit of U.S. Provisional Application No. 60 / 669,861, filed Apr. 7, 2005.TECHNICAL FIELD[0002]This invention is in the field of cancer-associated genes. Specifically it relates to methods for detecting cancer or the likelihood of developing cancer based on the presence or absence of PRLR gene expression or proteins encoded by this gene. The invention also provides methods and molecules for upregulating or downregulating the PRLR gene. In addition, the invention provides methods and molecules for the treatment of cancer, as well as methods of screening for molecules useful for the treatment of cancer.BACKGROUND OF THE INVENTION[0003]Oncogenes are genes that can cause cancer. Carcinogenesis can occur by a wide variety of mechanisms, including infection of cells by viruses containing oncogenes, activation of protooncogenes (normal genes that have the potential to become an oncogene) in the host genome, and mutations of protooncogenes and tumour suppr...

Claims

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Application Information

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IPC IPC(8): A61K39/395C12Q1/68C07K16/18C12N15/12C07K14/47A61K38/16A61K31/7105A61K31/7088A61P35/00
CPCC12Q1/6886C12Q2600/158C12Q2600/136C12Q2600/106A61P35/00
Inventor FANIDI, ABDALLAHBOOHER, ROBERTTSE, CHRISTIN
Owner FANIDI ABDALLAH
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